Yin Jun, Hu Bin, He Man, Jiang Zucheng
Department of Chemistry, Wuhan University, Wuhan 430072, PR China.
Anal Chim Acta. 2007 Jun 26;594(1):61-8. doi: 10.1016/j.aca.2007.05.011. Epub 2007 May 13.
Synergistic extraction of trace rare earth elements (REEs) from nitrate solutions using mixtures of dimethylheptyl methyl phosphate (P350) and 1-phenyl-3-methyl-4-benzoyl-pyrazalone-5 (PMBP) in hexamethylene has been investigated. The factors affecting the synergistic extraction of rare earth ions, such as pH, organic solvent and phase ratio of organic phase to aqueous phase were systematically studied. The synergistic enhancement factors of P350 and PMBP for REEs were calculated to be 4.3-5.8. After the synergistic extraction, the postextraction organic phase was directly introduced into the graphite furnace for electrothermal vaporization inductively coupled plasma mass spectrometry (ETV-ICP-MS) determination. It was found that PMBP along with P350 has an obvious chemical modification for REEs, and the limits of detection (LODs) for 15 REEs were in the range of 0.02-0.09 ng L(-1). The proposed method was found to be more suitable for the analysis of environmental samples with complex matrix.
研究了在己烷中使用磷酸二甲基庚酯(P350)和1-苯基-3-甲基-4-苯甲酰基吡唑啉酮-5(PMBP)混合物从硝酸盐溶液中协同萃取痕量稀土元素(REEs)的情况。系统研究了影响稀土离子协同萃取的因素,如pH值、有机溶剂以及有机相与水相的相比。计算得出P350和PMBP对REEs的协同增强因子为4.3 - 5.8。协同萃取后,将萃取后的有机相直接引入石墨炉进行电热蒸发电感耦合等离子体质谱(ETV-ICP-MS)测定。结果发现,PMBP与P350一起对REEs具有明显的化学修饰作用,15种REEs的检测限(LODs)在0.02 - 0.09 ng L⁻¹范围内。该方法被发现更适合分析具有复杂基质的环境样品。